http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0238554-A4

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-127
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-127
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-70
filingDate 1986-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f7a4950454dc2bba54fc9d90f1ef7ff5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c1d38fb41fb284c21cedc7880a200a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30382a93093c7f8627534b5c743f39c6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca645b1c49ab6adf4149c842959ebe81
publicationDate 1987-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0238554-A4
titleOfInvention LIPOSOME SYSTEM FOR TRANSDERMAL DRUG ADMINISTRATION.
abstract A transdermal drug release device for releasing a physiologically active, lipophilic drug to a skin surface at a selected, substantially constant rate over a period of at least about 24 hours. The device includes an aqueous-phase matrix having a surface adapted to be placed against the skin surface, and, embedded within the matrix, liposomes containing the drug in entrapped form and composed of lipid components which are selected to produce such drug release rate. In one embodiment, the matrix contains a water-soluble drug in free form, and then entrapped lipophilic drug is a drug transport agent designed to facilitate transdermal uptake of the water-soluble drug.
priorityDate 1985-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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